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Europe Approves Biogen's Tofersen For Adult Patients With Rare Type Of Neurodegenerative Disorder

Published 31/05/2024, 15:25
© Reuters.  Europe Approves Biogen\'s Tofersen For Adult Patients With Rare Type Of Neurodegenerative Disorder
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Benzinga - by Vandana Singh, Benzinga Editor.

On Thursday, the European Commission granted marketing authorization under exceptional circumstances and maintained orphan designation for Biogen Inc’s (NASDAQ:BIIB) Qalsody (tofersen) for amyotrophic lateral sclerosis (ALS) associated with a mutation in the superoxide dismutase 1 gene (SOD1-ALS).

Qalsody is the first treatment approved in the European Union to target a genetic cause of ALS, also known as motor neuron disease (MND).

SOD1-ALS is an ultra-rare genetic form of ALS estimated to affect less than 1,000 people in Europe.

Qalsody is Biogen’s third rare disease therapy to be approved in the EU.

Related: Tale Of Two Ionis-Partnered Neurology-Focused Early Stage Assets-Biogen Discontinues One, Decides Not To Exercise Licensing Option For Another.

In the Phase 3 VALOR study (n=108), patients were randomized 2:1 to receive treatment with either Qalsody 100 mg (n=72) or placebo (n=36) for 24 weeks.

The primary efficacy endpoint was the change from baseline to Week 28 in the ALS Functional Ratings Scale-Revised total score.

The results numerically favored tofersen but were not statistically significant.

At Week 28, mean plasma neurofilament light chain (NfL), a marker of axonal injury and neurodegeneration, was reduced by 55% in the tofersen-treated participants (ITT), compared to a 12% increase with placebo.

About 330 people with SOD1-ALS have received Qalsody across 18 EU countries through the Biogen early access program.

Last April, the FDA granted accelerated approval for Qalsody. In 2023, the drug generated sales of $5.9 million.

Biogen licensed Qalsody from Ionis Pharmaceuticals Inc (NASDAQ:IONS) under a collaborative development and license agreement. Ionis discovered Qalsody.

In addition to the ongoing open-label extension of the Phase 3 VALOR study, Qalsody is being studied in the Phase 3 ATLAS study to evaluate whether Qalsody can delay clinical onset when initiated in presymptomatic individuals with a SOD1 genetic mutation and biomarker evidence of disease activity.

Price Action: BIIB shares are up 1.90% at $224.26 at the last check on Friday.

© 2024 Benzinga.com. Benzinga does not provide investment advice. All rights reserved.

Read the original article on Benzinga

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